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Benzenesulfonic acid, 2,4,6-tris(1-methylethyl)-, cycloheptylidenehydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75415-79-1

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75415-79-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75415-79-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,1 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75415-79:
(7*7)+(6*5)+(5*4)+(4*1)+(3*5)+(2*7)+(1*9)=141
141 % 10 = 1
So 75415-79-1 is a valid CAS Registry Number.

75415-79-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name cycloheptanone (2,4,6-triisopropylbenzenesulfonyl)hydrazone

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:75415-79-1 SDS

75415-79-1Downstream Products

75415-79-1Relevant academic research and scientific papers

Silicon-Directed Nazarov Reactions II. Preparation and Cyclization of β-Silyl-substituted Divinyl Ketones

Jones, Todd K.,Denmark, Scott E.

, p. 2377 - 2396 (2007/10/02)

Two general methods for the preparation of β-silyl-substituted divinyl ketones have been developed starting from either α,β-unsaturated aldehydes or simple ketones.Anhydrous FeCl3 induces the cyclization to cyclopentenones under mild conditions and in good yields with predictable and complete control over the position of the double bond in the five-membered ring.The observed effects of substituents on rate can be explained by a rate-determining cationic electrocyclization.Silyl substitution has been shown to retard the reaction.

NITRODESTANNYLATION. A NEW SYNTHESIS OF CONJUGATED NITRO CYCLO OLEFINS

Corey, E. J.,Estreicher, Herbert

, p. 1113 - 1116 (2007/10/02)

A new process for the conversion of cyclic ketones to 1-nitro olefines, as outlined in eq. 2 below, is described.

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